Evolutionary islands in the Andes: persistence and isolation explain high endemism in Andean dry tropical forests

By T. Särkinen, R. Pennington, M. Lavin, M. Simon, C. Hughes. 2012

204 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/70456ada0f3d67f736306c887177ff27539b031e

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In Ecology, Evolution, Behavior and Systematics

In Nature and Landscape Conservation

Citations in the corpus

Phylogeny and biogeography in Solanaceae, Verbenaceae and Bignoniaceae: a comparison of continental and intercontinental diversification patterns (2013, background): “…recent physiographic province in South America (Antonelli et al., 2009; Antonelli & Sanmartin, 2011), there is both phylogenetic and fossil evidence for older plant diversification in the Andes, especially for Andean dry forest clades (Pennington et al., 2004, 2010; Särkinen et al., 2012).”
The emerging field of geogenomics: Constraining geological problems with genetic data (2014, background): “The latest phase of magmatism, focused in the Western Cordillera over the past ~30 Myr (Haschke et al., 2006), must have been associated with significant positive topography.”
Historical biogeography and life‐history evolution of Andean Puya (Bromeliaceae) (2013, background): “, 2009) and enable the incorporation of Puya into meta-analyses of the biota of the Andes (Hoorn et al., 2010; Antonelli & Sanmartín, 2011; Rull, 2011; Särkinen et al., 2011; Sklenář et al., 2011), further enhancing our understanding of the importance of geological events in the Cenozoic.”
Topography-driven isolation, speciation and a global increase of endemism with elevation (Forthcoming) (2016, unknown): “, 2012); phylogenetic research provides qualified support (Särkinen et al., 2012), and there are examples of the ancestors of tropical lowland lineages being montane (e.”
Phylogenetic insights into Andean plant diversification (2014, background): “The crown node of the genus Poissonia (Fabaceae) was dated to the Early Miocene (∼ 20 Ma; Pennington et al., 2004; Särkinen et al., 2011).”
Vulnerability of global biodiversity hotspots to climate change (2021, background): “By providing different combinations of slope and aspect, and by altering local weather patterns, topographical complexity has been found to play a crucial role in the diversification of different species clades (Rangel et al., 2018; Särkinen et al., 2012).”
Neotropical Plant Evolution: Assembling the Big Picture (2013, background): “, 2012a), and led to the emergence of the high elevation Andean grassland biomes with many spectacular examples of rapid plant species diversification (Hughes & Eastwood, 2006), several of which are documented here (Drew & Sytsma, 2012; Jabaily & Sytsma, 2012), as well as the deeper isolation of int”
Reconstructing the deep-branching relationships of the papilionoid legumes (2013, unknown): “The highly resolved Ateleioid phylogeny represents a common pattern in legumes with predilection to the succulent biome (e.g., Pennington et al., 2009, 2010; de Queiroz and Lavin, 2011; Särkinen et al., 2012),which contrasts to the low resolutionwithin the Swartzia clade andwhich is taken as evidenc”